Pirfenidone therapy and inducers of of cytochrome p450

ABSTRACT

The present invention relates to methods involving avoiding adverse drug interactions with pirfenidone and CYP inducers, such as smoking.

FIELD OF THE INVENTION

The invention relates to improved methods of administering pirfenidonetherapy, involving increased effectiveness of pirfenidone through theavoidance of inducers of cytochrome P450 (CYP) proteins which metabolizepirfenidone. More specifically, the invention is related to methods ofadministering pirfenidone therapy involving the avoidance of inducers ofCYP1A2.

BACKGROUND

Pirfenidone is small drug molecule whose chemical name is5-methyl-1-phenyl-2-(1H)-pyridone. It is a non-peptide syntheticmolecule with a molecular weight of 185.23 daltons. Its chemicalelements are expressed as C₁₂H₁₁NO, and its structure and synthesis areknown. Pirfenidone is manufactured commercially and being evaluatedclinically as a broad-spectrum anti-fibrotic drug. Pirfenidone hasanti-fibrotic properties via: decreased TGF-β expression, decreasedTNF-α expression, decreased PDGF expression, and decreased collagenexpression.

Pirfenidone is being investigated for therapeutic benefits to patientssuffering from fibrosis conditions such as Hermansky-Pudlak Syndrome(HPS) associated pulmonary fibrosis and idiopathic pulmonary fibrosis(IPF). Pirfenidone is also being investigated for a pharmacologicability to prevent or remove excessive scar tissue found in fibrosisassociated with injured tissues including that of lungs, skin, joints,kidneys, prostate glands, and livers. Published and unpublished basicand clinical research suggests that pirfenidone may safely slow orinhibit the progressive enlargement of fibrotic lesions, and preventformation of new fibrotic lesions following tissue injuries.

As an investigational drug, pirfenidone is provided in tablet andcapsule forms principally for oral administration. Various formulationshave been tested and adopted in clinical trials and other research andexperiments. The most common adverse reactions or events associated withpirfenidone therapy (>10%) are nausea, rash, dyspepsia, dizziness,vomiting, and photosensitivity reaction, and anorexia. Many of theseeffects can interfere with everyday activities and quality of life.These effects appear to be dose related. The adverse reactionsassociated with pirfenidone therapy are exacerbated when pirfenidone isadministered at higher doses. In comparison to studies performed todetermine the effects of pirfenidone therapy on patients, relativelylittle was known about the effects of pirfenidone when used incombination with other therapeutics.

Pirfenidone has been shown to be metabolized by isoforms of thecytochrome P450 (CYP) protein (Report on the Deliberation Results,Evaluation and Licensing Division, Pharmaceutical and Food SafetyBureau, Ministry of Health Labour and Welfare, Sep. 16, 2008).Specifically, several CYP isoforms (CYP1A2, 2C9, 2C19, 2D6 and 2E1) wereinvolved in the earliest stages of oxidative metabolism of pirfenidone.

Activity of CYPs in patients who smoke is significantly increased overtheir non-smoking counterparts.

SUMMARY

The invention disclosed herein is based upon the discovery of an adversereaction (reduced pirfenidone exposure) in patients taking pirfenidonewho also smoke.

The invention generally relates to improved methods of administeringpirfenidone to a patient in need of pirfenidone therapy, and to methodsof preparing or packaging pirfenidone medicaments, containers, packagesand kits. In any of the aspects or embodiments, the patient can haveidiopathic pulmonary fibrosis (IPF) and the medicament is for treatmentof IPF. In any of the aspects or embodiments, the therapeuticallyeffective amount of pirfenidone being administered can be a daily dosageof at least 1800 mg, or 2400 mg or 2403 mg per day. In any of theaspects of the invention, the daily dosage can be administered individed doses three times a day, or two times a day, or alternatively isadministered in a single dose once a day. In any of the aspects of theinvention, the pirfenidone can be administered with food. For example,the daily dosage of 2400 mg or 2403 mg pirfenidone per day can beadministered as follows: 800 mg or 801 mg taken three times a day, withfood.

In some aspects, the invention provides a method of administeringpirfenidone therapy to a patient in need of pirfenidone therapy (e.g., apatient with IPF), involving administering to the patient atherapeutically effective amount of pirfenidone, and avoiding use oradministration of an inducer of a cytochrome P450 (CYP) that metabolizespirfenidone (“CYP inducer”). In some cases, the use or administration ofthe CYP inducer is avoided for at least 2.5 hours after administrationof the pirfenidone. In various cases, the CYP that metabolizespirfenidone is cytochrome P450 1A2 (CYP1A2). In some embodiments, theCYP inducer is a strong CYP1A2 inducer. Induction of CYP1A2 activity hasbeen reported as a consequence of cigarette smoking, dietary factors,several drugs, chronic hepatitis, and exposure to polybrominatedbiphenyls and 2,3,7,8-tetrachlorodibenzo-p-dioxin. Landi et al. IARC SciPubl. 1999; (148):173-95. In addition to, or in the alternative tosmoking, the CYP inducers to be discontinued or avoided can be selectedfrom the group consisting of carbamazepine, esomeprazole, griseofulvin,insulin, lansprazole, moricizine, omeprazole, rifampin, and ritonavir.The CYP inducers to be discontinued or avoided can additionally oralternatively be charbroiled foods and/or cruciferous vegetables. TheCYP inducers to be discontinued or avoided can additionally oralternatively be selected from the group consisting of phenobarbital,phenyloin, primidone, and St. John's wort.

In other aspects, the invention provides a method of administeringpirfenidone therapy to a patient in need of pirfenidone therapy,comprising discontinuing use or administration of an inducer of a CYPthat metabolizes pirfenidone, e.g. a strong CYP1A2 inducer, to avoid anadverse drug interaction (e.g. or to avoid reduced exposure topirfenidone) and administering a therapeutically effective amount ofpirfenidone. In one embodiment, the patient discontinues use oradministration of the CYP inducer concurrent with startingadministration of pirfenidone. In another embodiment, the use oradministration of the CYP inducer is discontinued within at least 3 daysto within 4 weeks prior to or after starting pirfenidone therapy. Thistime period can, for example, permit adequate time for tapering andwithdrawal without adverse effects, if such tapering is useful for theCYP inducer. In one example, in a method of administering atherapeutically effective amount of pirfenidone to a patient with IPF,the invention provides an improvement that comprises avoiding ordiscontinuing administration of a CYP inducer that metabolizespirfenidone and administering a therapeutically effective amount ofpirfenidone. In some embodiments, when the patient is a smoker (e.g.,has not quit smoking), the patient avoids smoking for at least 2.5 hoursafter administration of pirfenidone.

In some embodiments, the patient is a smoker who is discontinuingsmoking. In various embodiments, the method or use further comprisesadministering to the smoker patient a nicotine replacement therapy orother smoking cessation therapy. The nicotine replacement therapy cancomprise one or more of a nicotine patch, a nicotine gum, a nicotinelozenge, a nicotine nasal spray, and a nicotine inhaler. The method canadditionally or alternatively comprise administering buproprionhydrochloride (Zyban®) or varenciline (Chantix®).

Thus, an aspect of the invention provides pirfenidone for use intreating a patient in need of pirfenidone therapy, characterized in thatthe treating comprises avoiding, discontinuing, or contraindicatingconcomitant use or co-administration of a strong inducer of cytochromeP450 1A2 (CYP1A2). The concomitant use or co-administration is avoided,discontinued or contraindicated, in order to avoid the reduced(decreased) exposure to pirfenidone, or the potential for reducedexposure to pirfenidone. Administration of pirfenidone in patients thatconcomitantly smoke results in about 50% decrease in pirfenidoneexposure (AUC_(O-∞)), on average, compared to patients that do notsmoke. It is understood that any of the aspects or embodiments orexamples described herein with respect to methods of treatment apply tothis aspect of the invention that provides pirfenidone for use intreating a patient. For example, the patient may be a patient with IPF,and the therapeutically effective amount administered may be at least1800 mg, or 2400 or 2403 mg per day. As another example, the strongCYP1A2 inducer may be any known in the art or any of the strong CYP1A2inducers described herein.

Similarly, a further related aspect of the invention provides the use ofpirfenidone in the manufacture of a medicament for treating a patient inneed of pirfenidone therapy, characterized in that the treatingcomprises avoiding, discontinuing, or contraindicating concomitant useor co-administration of a strong inducer of cytochrome P450 1A2 (CYP1A2)to avoid reduced exposure to pirfenidone. It is understood that any ofthe aspects or embodiments or examples described herein with respect tomethods of treatment apply to this aspect of the invention that providesfor the use of pirfenidone in manufacture of a medicament. For example,the patient may be a patient with IPF, and the therapeutically effectiveamount administered may be at least 1800 mg, or, more specifically 2400or 2403 mg per day. As another example, the strong CYP1A2 inducer may beany known in the art or any of the strong CYP1A2 inducers describedherein.

As used herein, “concomitant use” is understood to be interchangeablewith concurrent administration or co-administration. Thus, the terms areunderstood to encompass administration simultaneously, or at differenttimes, and by the same route or by different routes, as long as the twoagents are given in a manner that allows both agents to be affecting thebody at the same time. For example, concomitant use can refer to amedication concomitantly administered, whether prescribed by the same ora different practitioner, or for the same or a different indication.

In some embodiments, the patient is a patient in need of therapy with aCYP1A2 inducer, e.g. a strong CYP1A2 inducer. In some embodiments, thepatient is a patient who was or is a smoker. In some embodiments, thepatient is a patient who was a smoker immediately prior to startingadministration of pirfenidone. In some embodiments, the patient in needof pirfenidone therapy is a patient avoiding concomitant use orco-administration of a strong inducer of cytochrome P450 1A2 (CYP1A2).In some embodiments, the patient is a patient who has been or is asmoker, and the patient is avoiding smoking when using pirfenidone. Insome embodiments, the patient in need of pirfenidone therapy is a smokerwho is discontinuing smoking to avoid reduced exposure to pirfenidone.In exemplary embodiments, the patient discontinues smoking within 4weeks prior to the administration of pirfenidone, or concurrent with thestart of administration of pirfenidone. It is understood that any of theaspects or embodiments or examples described herein with respect tomethods of treatment apply to this aspect of the invention that providesfor characterization of the patients to be treated with pirfenidone.

In yet other aspects, a method of administering pirfenidone therapy to apatient in need of pirfenidone comprises administering a therapeuticallyeffective amount of pirfenidone to the patient, and any one, two, three,or more of the following:

-   -   (a) advising the patient that CYP inducers that metabolize        pirfenidone should be avoided or discontinued or that inducers        of CYP that metabolize pirfenidone are contraindicated;    -   (b) advising the patient that smoking should be avoided or        discontinued;    -   (c) advising the patient that co-administration of pirfenidone        with a CYP inducer that metabolizes pirfenidone can alter the        therapeutic effect of pirfenidone;    -   (d) advising the patient that administration of pirfenidone in        patients that smoke results in a 50% decrease in pirfenidone        exposure compared to patients that do not smoke; and    -   (e) advising the patient that smoking may result in decreased        pirfenidone exposure due to the potential for smoking to induce        CYP1A2 metabolism.

For the patient who smokes, the method can further comprise advising thepatient to consider nicotine replacement therapy in place of smokingand/or encouraging the patent to stop smoking before treatment withpirfenidone.

In some embodiments, a method of reducing toxicity of pirfenidonetreatment in a patient is provided comprising administering atherapeutically effective amount of pirfenidone to the patient andadvising the patient of any of the foregoing advice.

In some embodiments, a method of improving safety of pirfenidonetreatment in a patient is provided comprising administering atherapeutically effective amount of pirfenidone to the patient andadvising the patient of any of the foregoing advice.

In some embodiments, a method of reducing adverse drug interaction withpirfenidone treatment in a patient (e.g., to avoid reduced exposure topirfenidone) is provided, comprising administering a therapeuticallyeffective amount of pirfenidone to the patient and advising the patientof any of the foregoing advice.

Thus, in some embodiments, the concomitant use or co-administration ofstrong CYP1A2 inducers is avoided, discontinued, or contraindicated inorder to

-   -   (a) avoid the potential for the altered therapeutic effect of        pirfenidone, and/or    -   (b) avoid the reduced exposure or potential for reduced        exposure, and/or    -   (c) reduce toxicity of pirfenidone treatment, and/or    -   (d) improve safety of pirfenidone treatment, and/or    -   (e) reduce adverse drug interaction associated with pirfenidone        treatment.

In some embodiments, smoking is avoided, discontinued, orcontraindicated in order to avoid the 50% decrease in pirfenidoneexposure compared to patients that do not smoke.

BRIEF DESCRIPTION OF THE FIGURE

FIG. 1 depicts a symmetrical dot plot of AUC_(0-∞) estimates by studyday—circles indicate smokers, triangles indicate nonsmokers.

DETAILED DESCRIPTION

Pirfenidone is an orally active, anti-fibrotic agent. Results of invitro experiments indicated that pirfenidone is primarily metabolized byCYP1A2 (approx. 48%) with multiple other CYPs contributing as well (each<13%) (i.e., 1A1, 2A6, 2B6, 2C8, 2C9, 2C18, 2C19, 2D6, 2E1, 2J2, 3A4,3A5, 4A11, and 4F2). Oral administration of pirfenidone results in theformation of four metabolites, 5 hydroxymethyl-pirfenidone, 5carboxy-pirfenidone, 4′-hydroxy-pirfenidone, and the 50-acyl glucuronidemetabolite of 5 carboxy-pirfenidone. In humans, only pirfenidone and5-carboxy-pirfenidone are present in plasma in significant quantities;none of the other metabolites occur in sufficient quantities to allowfor PK analysis. There are no unique human metabolites.

The terms “therapeutically effective amount,” as used herein, refer toan amount of a compound sufficient to treat, ameliorate, or prevent theidentified disease or condition, or to exhibit a detectable therapeutic,prophylactic, or inhibitory effect. The effect can be detected by, forexample, an improvement in clinical condition, or reduction in symptoms.The precise effective amount for a subject will depend upon thesubject's body weight, size, and health; the nature and extent of thecondition; and the therapeutic or combination of therapeutics selectedfor administration.

As used herein, a patient “in need of pirfenidone therapy” is a patientwho would benefit from administration of pirfenidone. The patient may besuffering from any disease or condition for which pirfenidone therapymay be useful in ameliorating symptoms. Such diseases or conditionsinclude pulmonary fibrosis, idiopathic pulmonary fibrosis, idiopathicinterstitial pneumonia, autoimmune lung diseases, benign prostatehypertrophy, coronary or myocardial infarction, atrial fibrillation,cerebral infarction, myocardiac fibrosis, musculoskeletal fibrosis,post-surgical adhesions, liver cirrhosis, renal fibrotic disease,fibrotic vascular disease, scleroderma, Hermansky-Pudlak syndrome,neurofibromatosis, Alzheimer's disease, diabetic retinopathy, and/orskin lesions, lymph node fibrosis associated with HIV, chronicobstructive pulmonary disease (COPD), inflammatory pulmonary fibrosis,rheumatoid arthritis; rheumatoid spondylitis; osteoarthritis; gout,other arthritic conditions; sepsis; septic shock; endotoxic shock;gram-negative sepsis; toxic shock syndrome; myofacial pain syndrome(MPS); Shigellosis; asthma; adult respiratory distress syndrome;inflammatory bowel disease; Crohn's disease; psoriasis; eczema;ulcerative colitis; glomerular nephritis; scleroderma; chronicthyroiditis; Grave's disease; Ormond's disease; autoimmune gastritis;myasthenia gravis; autoimmune hemolytic anemia; autoimmune neutropenia;thrombocytopenia; pancreatic fibrosis; chronic active hepatitisincluding hepatic fibrosis; acute and chronic renal disease; renalfibrosis; diabetic nephropathy; irritable bowel syndrome; pyresis;restenosis; cerebral malaria; stroke and ischemic injury; neural trauma;Alzheimer's disease; Huntington's disease; Parkinson's disease; acuteand chronic pain; allergies, including allergic rhinitis and allergicconjunctivitis; cardiac hypertrophy, chronic heart failure; acutecoronary syndrome; cachexia; malaria; leprosy; leishmaniasis; Lymedisease; Reiter's syndrome; acute synoviitis; muscle degeneration,bursitis; tendonitis; tenosynoviitis; herniated, ruptured, or prolapsedintervertebral disk syndrome; osteopetrosis; thrombosis; silicosis;pulmonary sarcosis; bone resorption diseases, such as osteoporosis ormultiple myeloma-related bone disorders; cancer, including but notlimited to metastatic breast carcinoma, colorectal carcinoma, malignantmelanoma, gastric cancer, and non-small cell lung cancer;graft-versus-host reaction; and auto-immune diseases, such as multiplesclerosis, lupus and fibromyalgia; AIDS and other viral diseases such asHerpes Zoster, Herpes Simplex I or II, influenza virus, Severe AcuteRespiratory Syndrome (SARS) and cytomegalovirus; and diabetes mellitus.In addition, the methods of the embodiments can be used to treatproliferative disorders (including both benign and malignanthyperplasias), including acute myelogenous leukemia, chronic myelogenousleukemia, Kaposi's sarcoma, metastatic melanoma, multiple myeloma,breast cancer, including metastatic breast carcinoma; colorectal.carcinoma; malignant melanoma; gastric cancer; non-small cell lungcancer (NSCLC); bone metastases, and the like; pain disorders includingneuromuscular pain, headache, cancer pain, dental pain, and arthritispain; angiogenic disorders including solid tumor angiogenesis, ocularneovascularization, and infantile hemangioma; conditions associated withthe cyclooxygenase and lipoxygenase signaling pathways, includingconditions associated with prostaglandin endoperoxide synthase-2(including edema, fever, analgesia, and pain); organ hypoxia;thrombin-induced platelet aggregation; protozoal diseases.

As used herein, the term “avoid” and forms thereof are contemplated tohave as alternatives the terms abstain, desist, forbear, and refrain,and forms thereof. As used herein, the term “discontinue” and formsthereof are contemplated to have as alternatives the terms cease, stop,suspend, and quit.

Preferably, a CYP inducer that metabolizes pirfenidone or a stronginducer of CYP1A2 is one that decreases plasma AUC values of pirfenidoneby 30% or more. A strong CYP inducer that metabolizes pirfenidone, e.g.,a strong inducer of CYP1A2, is preferably one that decreases plasma AUCvalues of pirfenidone by 50% or more.

In some embodiments, the effect of a CYP inducer on metabolism ofpirfenidone in an individual patient is normalized based upon thepatient's body surface area (BSA). BSA can be calculated using apatient's height and weight. In specific embodiments, the normalizedeffect of the CYP inducer is an at least 30% or at least 50% decrease inAUC values of pirfenidone.

CYP Inducers

In any of the embodiments described herein, including but not limited tothe pirfenidone for use in treating a patient, the use of pirfenidone inthe manufacture of a medicament for treating a patient in need ofpirfenidone therapy, treatment methods involving the advice, warnings,discontinuation or dose titration downwards, the packages and kits,and/or the methods of preparing or packaging pirfenidone, thepirfenidone, uses, methods, packages, kits, advice, warnings,discontinuation or dose titration may apply not only to smoking but alsoto any other activity or drug that induces a CYP that metabolizespirfenidone, including CYP1A2. The CYP inducer can be charbroiled meatsor cruciferous vegetables. Additionally or alternatively, the CYPinducer can be one or more of phenobarbital, phenyloin, primidone, orSt. John's wort. Additionally or alternatively, the CYP inducer can beone or more of carbamazepine, esomeprazole, griseofulvin, insulin,lansprazole, moricizine, omeprazole, rifampin, or ritonavir.

Avoiding, Discontinuing or Contraindicating Administration of a CYPInducer to Avoid Adverse Drug Interactions with Pirfenidone (E.G., toAvoid Reduced Exposure to Pirfenidone)

In some aspects, the invention provides a method of administeringpirfenidone therapy to a patient in need of pirfenidone therapy orpirfenidone for use in treating a patient in need of pirfenidone therapy(e.g., a patient with IPF), involving administering to the patient atherapeutically effective amount of pirfenidone, and avoiding use oradministration (e.g., concomitant use or co-administration) of a CYPinducer that metabolizes pirfenidone (e.g., CYP1A2). In someembodiments, the CYP inducer is smoking (e.g., inhalation of the smokeof burning organic material, particularly tobacco or marijuana), as theresult of polycyclic aromatic hydrocarbons which are contained in suchsmoke.

In other aspects, the invention provides a method of administeringpirfenidone therapy to a patient in need of pirfenidone therapy, orpirfenidone for use in treating a patient in need of pirfenidonetherapy, comprising discontinuing administration (e.g.co-administration) of a drug that is a CYP1A2 inducer to avoid anadverse drug interaction (e.g., to avoid reduced exposure topirfenidone), and administering a therapeutically effective amount ofpirfenidone.

In one example, in a method of administering a therapeutically effectiveamount of pirfenidone to a patient with IPF, or pirfenidone for use intreating a patient in need of pirfenidone therapy, the inventionprovides an improvement that comprises avoiding or discontinuingadministration (e.g., concomitant use or co-administration) of a CYPinducer and administering a therapeutically effective amount ofpirfenidone.

In some embodiments, the CYP inducer is discontinued concurrent withstarting administration of pirfenidone. In other embodiments, the CYPinducer is discontinued within at least 3 days prior to startingpirfenidone therapy. In another embodiment, the CYP inducer can bediscontinued within up to 4 weeks prior to starting pirfenidone therapy.In another embodiment, the CYP inducer is discontinued within 3 daysafter starting pirfenidone therapy, optionally up to 4 weeks afterstarting pirfenidone therapy. These time periods, for example, canpermit adequate time for tapering and withdrawal without adverseeffects.

In embodiments in which the CYP inducer is discontinued to avoid anadverse drug interaction (e.g., to avoid reduced exposure topirfenidone), the CYP inducer preferably is discontinued within at least3 days prior to starting pirfenidone therapy. In various embodiments,the CYP inducer is discontinued within at least 4 days, or at least 5days, or at least 6 days, or at least 7 days (or one week), or at least8 days, or at least 9 days, or at least 10 days, or at least 11 days, orat least 12 days, or at least 13 days, or at least 14 days (or twoweeks), or at least 15 days, or at least 16 days, or at least 17 days,or at least 18 days, or at least 19 days, or at least 20 days, or atleast 21 days (or three weeks), or at least 22 days, or at least 23days, or at least 24 days, or at least 25 days, or at least 26 days, orat least 27 days, or at least 28 days (or four weeks), or at least 29days, or at least 30 days, or at least one month, prior to startingpirfenidone therapy. In some embodiments, the CYP inducer isdiscontinued no earlier than one month, 3 weeks, 2 weeks or 1 weekbefore starting pirfenidone therapy. Preferably, sufficient time isallowed for tapering and/or withdrawal of the CYP inducer.

In embodiments where the CYP inducer cannot be or is not discontinuedprior pirfenidone therapy, the CYP inducer is preferably discontinuedwithin at least 3 days after starting pirfenidone therapy. In variousembodiments, the CYP inducer is discontinued within at least 4 days, orat least 5 days, or at least 6 days, or at least 7 days (or one week),or at least 8 days, or at least 9 days, or at least 10 days, or at least11 days, or at least 12 days, or at least 13 days, or at least 14 days(or two weeks), or at least 15 days, or at least 16 days, or at least 17days, or at least 18 days, or at least 19 days, or at least 20 days, orat least 21 days (or three weeks), or at least 22 days, or at least 23days, or at least 24 days, or at least 25 days, or at least 26 days, orat least 27 days, or at least 28 days (or four weeks), or at least 29days, or at least 30 days, or at least one month, after startingpirfenidone therapy. In some embodiments, the CYP inducer isdiscontinued no later than one month, 3 weeks, 2 weeks or 1 week afterstarting pirfenidone therapy.

In embodiments in which the patient discontinues smoking to avoid anadverse drug interaction (e.g., to avoid reduced exposure topirfenidone), the smoking preferably is discontinued within at least 3days prior to starting pirfenidone therapy. In various embodiments, thepatient discontinues smoking within at least 4 days, or at least 5 days,or at least 6 days, or at least 7 days (or one week), or at least 8days, or at least 9 days, or at least 10 days, or at least 11 days, orat least 12 days, or at least 13 days, or at least 14 days (or twoweeks), or at least 15 days, or at least 16 days, or at least 17 days,or at least 18 days, or at least 19 days, or at least 20 days, or atleast 21 days (or three weeks), or at least 22 days, or at least 23days, or at least 24 days, or at least 25 days, or at least 26 days, orat least 27 days, or at least 28 days (or four weeks), or at least 29days, or at least 30 days, or at least one month, prior to startingpirfenidone therapy. In some embodiments, the patient discontinuessmoking no earlier than one month, 3 weeks, 2 weeks or 1 week beforestarting pirfenidone therapy. Preferably, sufficient time is allowed fortapering and/or withdrawal of the smoking.

In embodiments in which the patient cannot or does not discontinuesmoking prior to pirfenidone therapy, the smoking preferably isdiscontinued within at least 3 days after starting pirfenidone therapy.In various embodiments, the patient discontinues smoking within at least4 days, or at least 5 days, or at least 6 days, or at least 7 days (orone week), or at least 8 days, or at least 9 days, or at least 10 days,or at least 11 days, or at least 12 days, or at least 13 days, or atleast 14 days (or two weeks), or at least 15 days, or at least 16 days,or at least 17 days, or at least 18 days, or at least 19 days, or atleast 20 days, or at least 21 days (or three weeks), or at least 22days, or at least 23 days, or at least 24 days, or at least 25 days, orat least 26 days, or at least 27 days, or at least 28 days (or fourweeks), or at least 29 days, or at least 30 days, or at least one month,after starting pirfenidone therapy. In some embodiments, the patientdiscontinues smoking no later than one month, 3 weeks, 2 weeks or 1 weekafter starting pirfenidone therapy.

The patient preferably avoids use of the CYP inducer to allow sufficienttime for the full dose of pirfenidone to be substantially absorbed bythe patient's body. Pirfenidone has a serum half life in humans of about2 to 3 hours. Thus, the patient preferably avoids use of the CYPinducer, for example, for at least 2.5 hours after administration of thepirfenidone. The patient can also avoid use of the CYP inducer for atleast 3 hours, at least 3.5 hours, at least 4 hours, at least 4.5 hours,or at least 5 hours after administration of the pirfenidone. For examplein embodiments where the patient is a smoker, the patient can avoidsmoking for at least 2.5 hours, at least 3 hours, at least 3.5 hours, atleast 4 hours, at least 4.5 hours, or at least 5 hours afteradministration of the pirfenidone. Similarly, the patient preferablyavoids use of the CYP inducer for at least 1, 2, 3, or 4 seriumhalf-lives of the CYP inducer prior to use of pirfenidone.

Selecting an Alternative Drug or Therapy to Administer Concurrently withPirfenidone Therapy

In some aspects, the invention provides a method of administeringpirfenidone therapy to a patient in need of pirfenidone therapy and inneed of therapy with a drug that is a CYP inducer, such as an inducer ofCYP1A2, comprising administering a therapeutically effective amount ofpirfenidone to the patient, and administering an alternative therapythat is not a CYP inducer.

In other aspects, the invention provides a method of administeringpirfenidone therapy to a patient who smokes and in need of pirfenidonetherapy, comprising administering a therapeutically effective amount ofpirfenidone to the patient, and administering a stop-smoking therapy,for example nicotine replacement therapy. The nicotine replacementtherapy can be any nicotine source and can include a nicotine patch, anicotine gum, a nicotine lozenge, a nicotine nasal spray, and a nicotineinhaler. Additionally or alternatively, the method can includeadministration of a drug to assist in smoking cessation. Non-limitingexamples of smoking cessation drugs include, but are not limited to,bupropion hydrochloride (Zyban®) or varenicline (Chantix®).

Improving Administration of Pirfenidone by Advising or CautioningPatient

The administration of a therapeutically effective amount of pirfenidoneto a patient in need of pirfenidone therapy can be improved. In someembodiments, the patient is advised that co-administration ofpirfenidone with a CYP inducer that metabolizes pirfenidone can alterthe therapeutic effect or adverse reaction profile of pirfenidone (e.g.,can reduce exposure to pirfenidone). In some embodiments, the patient isadvised that administration of pirfenidone and smoking can alter thetherapeutic effect or adverse reaction profile of pirfenidone (e.g., canreduce exposure to pirfenidone).

In some embodiments, the patient is advised that co-administration ofpirfenidone with a drug that is a CYP1A2 inducer can alter thetherapeutic effect or adverse reaction profile of pirfenidone (e.g., canreduce exposure to pirfenidone). In some embodiments, the patient isadvised that co-administration of pirfenidone with a CYP1A2 inducer canalter the therapeutic effect or adverse reaction profile of pirfenidone(e.g., can reduce exposure to pirfenidone).

In some embodiments, the patient is advised that use of pirfenidone inpatients who smoke can alter the therapeutic effect or adverse reactionprofile of pirfenidone (e.g., can reduce exposure to pirfenidone). Insome embodiments, the patient is advised that use of pirfenidone inpatients who smoke resulted in or can result in a 50% decrease inexposure to pirfenidone.

Dosing and Dose Modifications

In various embodiments, a method of administering pirfenidone and a CYPinducer that metabolizes pirfenidone (e.g., CYP1A2) is provided whereinthe patient is administered a therapeutically effective amount of theinducer and a dosage of pirfenidone that is increased relative to apatient not taking the inducer. In some aspects, such an increaseddosage of pirfenidone is greater than 2400 mg/day. For example, theincreased dosage is about 2670 mg per day, 2937 mg per day, 3204 mg perday, 3471 mg per day, or 3738 mg per day (e.g., 10, 11, 12, 13, or 14capsules per day where each capsule is approximately 267 mg), or higher.In another example, the dosage is increased from about 2400 mg or 2403mg per day to about 4800 mg or 4806 mg per day. In some embodiments, thepatient is already being administered the CYP inducer. In otherembodiments, the patient is already being administered pirfenidone. Inrelated embodiments, the dosage of pirfenidone is increased prior toadministration of the CYP inducer.

In embodiments wherein the patient avoids or discontinues use of the CYPinducer, preferably the amount of pirfenidone being administered is atleast 1800 mg, or 2400 or 2403 mg/day. Pirfenidone can be dosed at atotal amount of about 2400 mg to about 3800 mg or 4800 mg per day. Thedosage can be divided into two or three doses over the day or given in asingle daily dose. Specific amounts of the total daily amount of thetherapeutic contemplated for the disclosed methods include about 2400mg, about 2450 mg, about 2500 mg, about 2550 mg, about 2600 mg, about2650 mg, about 2670 mg, about 2700 mg, about 2750 mg, about 2800 mg,about 2850 mg, about 2900 mg, about 2937 mg, about 2950 mg, about 3000mg, about 3050 mg, about 3100 mg, about 3150 mg, about 3200 mg, about3204 mg, about 3250 mg, about 3300 mg, about 3350 mg, about 3400 mg,about 3450 mg, about 3471 mg, about 3500 mg, about 3550 mg, about 3600mg, about 3650 mg, about 3700 mg, about 3738 mg, about 3750 mg, andabout 3800 mg.

Dosages of pirfenidone can alternately be administered as a dosemeasured in mg/kg. Contemplated mg/kg doses of the disclosedtherapeutics include about 1 mg/kg to about 40 mg/kg. Specific ranges ofdoses in mg/kg include about 1 mg/kg to about 20 mg/kg, about 5 mg/kg toabout 20 mg/kg, about 10 mg/kg to about 20 mg/kg, about 10 mg/kg toabout 30 mg/kg, and about 15 mg/kg to about 25 mg/kg. Other specificranges of doses include about 1 mg/kg to about 35 mg/kg. Specific dosescontemplated include about 1 mg/kg, about 2 mg/kg, about 3 mg/kg, about4 mg/kg, about 5 mg/kg, about 6 mg/kg, about 7 mg/kg, about 8 mg/kg,about 9 mg/kg, about 10 mg/kg, about 11 mg/kg, about 12 mg/kg, about 13mg/kg, about 14 mg/kg, about 15 mg/kg, about 16 mg/kg, about 17 mg/kg,about 18 mg/kg, about 19 mg/kg, about 20 mg/kg, about 21 mg/kg, about 22mg/kg, about 23 mg/kg, about 24 mg/kg, about 25 mg/kg, about 26 mg/kg,about 27 mg/kg, about 28 mg/kg, about 29 mg/kg, about 30 mg/kg, about 31mg/kg, about 32 mg/kg, about 33 mg/kg, about 34 mg/kg, about 35 mg/kg,about 36 mg/kg, about 37 mg/kg, about 38 mg/kg, about 39 mg/kg, about 40mg/kg.

In one aspect of a use or method described herein, a dosage amount ofpirfenidone is taken with food. In another aspect, the patient isinstructed to administer the dosage of pirfenidone with food.

In some embodiments, a method of optimizing pirfenidone therapy isprovided comprising titrating the dosage of pirfenidone administered toa patient upward relative to a previously administered dosage in thepatient, wherein co-administration of a CYP inducer that metabolizespirfenidone to the patient does not result in a decreased exposure topirfenidone. In some embodiments, the dose is increased by about 100mg/day. In other embodiments, the dose is increased by about 150 mg/day,or about 200 mg/day, or about 250 mg/day, or about 267 mg/day, or about300 mg/day, or about 350 mg/day, or about 400 mg/day, or about 450mg/day, or about 500 mg/day, or about 550 mg/day, or about 600 mg/day,or about 650 mg/day, or about 700 mg/day, or about 750 mg/day, or about800 mg/day, or about 850 mg/day, or about 900 mg/day, or about 950mg/day, or about 1000 mg/day, or about 1050 mg/day, or about 1100mg/day, or about 1150 mg/day, or about 1200 mg/day, or about 1250mg/day, or about 1300 mg/day, or about 1350 mg/day, or about 1400mg/day, or about 1450 mg/day, or about 1500 mg/day, or about 1600mg/day, or about 1650 mg/day, or about 1700 mg/day, or about 1750mg/day, or about 1800 mg/day, or about 1850 mg/day, or about 1900mg/day, or about 1950 mg/day, or about 2000 mg/day, or about 2050mg/day, or about 2100 mg/day, or about 2150 mg/day, or about 2200mg/day, or about 2250 mg/day, or about 2300 mg/day, or about 2350mg/day, or about 2400 mg/day or more. For example, the dosage isincreased from about 2400 mg or 2403 mg per day to about 4800 mg or 4806mg per day. As another example, the dosage is increased from about 1800mg per day to about 3600 mg per day.

In some embodiments, a method of optimizing pirfenidone therapy isprovided comprising titrating the dosage of pirfenidone administered toa patient upward relative to a previously administered dosage in thepatient, wherein co-administration of a drug that is an inducer ofCYP1A2 to the patient does not result in a decreased exposure topirfenidone. In some embodiments, the dose is increased by about 100mg/day. In other embodiments, the dose is increased by about 150 mg/day,or about 200 mg/day, or about 250 mg/day, or about 267 mg/day, or about300 mg/day, or about 350 mg/day, or about 400 mg/day, or about 450mg/day, or about 500 mg/day, or about 550 mg/day, or about 600 mg/day,or about 650 mg/day, or about 700 mg/day, or about 750 mg/day, or about800 mg/day, or about 850 mg/day, or about 900 mg/day, or about 950mg/day, or about 1000 mg/day, or about 1050 mg/day, or about 1100mg/day, or about 1150 mg/day, or about 1200 mg/day, or about 1250mg/day, or about 1300 mg/day, or about 1350 mg/day, or about 1400mg/day, or about 1450 mg/day, or about 1500 mg/day, or about 1600mg/day, or about 1650 mg/day, or about 1700 mg/day, or about 1750mg/day, or about 1800 mg/day, or about 1850 mg/day, or about 1900mg/day, or about 1950 mg/day, or about 2000 mg/day, or about 2050mg/day, or about 2100 mg/day, or about 2150 mg/day, or about 2200mg/day, or about 2250 mg/day, or about 2300 mg/day, or about 2350mg/day, or about 2400 mg/day or more. For example, the dosage isincreased from about 2400 mg or 2403 mg per day to about 4800 mg or 4806mg per day. As another example, the dosage is increased from about 1800mg per day to about 3600 mg per day.

In some embodiments, a method of optimizing pirfenidone therapy isprovided comprising titrating the dosage of pirfenidone administered toa patient upward relative to a previously administered dosage in thepatient, wherein co-administration of a CYP1A2 inducer to the patientdoes not result in a decreased exposure to pirfenidone. In someembodiments, the dose is increased by about 100 mg/day. In otherembodiments, the dose is increased by about 150 mg/day, or about 200mg/day, or about 250 mg/day, or about 267 mg/day, or about 300 mg/day,or about 350 mg/day, or about 400 mg/day, or about 450 mg/day, or about500 mg/day, or about 550 mg/day, or about 600 mg/day, or about 650mg/day, or about 700 mg/day, or about 750 mg/day, or about 800 mg/day,or about 850 mg/day, or about 900 mg/day, or about 950 mg/day, or about1000 mg/day, or about 1050 mg/day, or about 1100 mg/day, or about 1150mg/day, or about 1200 mg/day, or about 1250 mg/day, or about 1300mg/day, or about 1350 mg/day, or about 1400 mg/day, or about 1450mg/day, or about 1500 mg/day, or about 1600 mg/day, or about 1650mg/day, or about 1700 mg/day, or about 1750 mg/day, or about 1800mg/day, or about 1850 mg/day, or about 1900 mg/day, or about 1950mg/day, or about 2000 mg/day, or about 2050 mg/day, or about 2100mg/day, or about 2150 mg/day, or about 2200 mg/day, or about 2250mg/day, or about 2300 mg/day, or about 2350 mg/day, or about 2400 mg/dayor more. For example, the dosage is increased from about 2400 mg or 2403mg per day to about 4800 mg or 4806 mg per day. As another example, thedosage is increased from about 1800 mg per day to about 3600 mg per day.

Packages, Kits, Methods of Packaging, and Methods of Delivering

In another aspect, a package or kit is provided comprising pirfenidone,optionally in a container, and a package insert, package label,instructions or other labeling including any one, two, three or more ofthe following information or recommendations:

-   -   (a) advising the patient that strong CYP inducers that        metabolize pirfenidone should be avoided or discontinued;    -   (b) advising the patient that smoking should be avoided or        discontinued;    -   (c) advising the patient that co-administration of pirfenidone        with a CYP inducer that metabolizes pirfenidone can alter the        therapeutic effect of pirfenidone;    -   (d) advising the patient that administration of pirfenidone in        patients that smoke results in a 50% decrease in pirfenidone        exposure compared to patients that do not smoke; and    -   (e) advising the patient that smoking may result in decreased        pirfenidone exposure due to the potential for smoking to induce        CYP1A2 metabolism. In some embodiments, the information or        recommendation may include that co-administration of pirfenidone        with inducers of CYP that metabolize pirfenidone can alter the        therapeutic effect or adverse reaction profile of pirfenidone        (e.g., can reduce exposure to pirfenidone). In other        embodiments, the information or recommendation may include that        administration of pirfenidone to a patient who smokes can alter        the therapeutic effect or adverse reaction profile of        pirfenidone (e.g., can reduce exposure to pirfenidone). In other        embodiments, the information or recommendation may include that        co-administration of pirfenidone with CYP1A2 inducers can alter        the therapeutic effect or adverse reaction profile of        pirfenidone (e.g., can reduce exposure to pirfenidone).

In other embodiments, the information or recommendation may include thatdrugs that are CYP1A2 inducers should be avoided. In other embodiments,the information or recommendation may include that drugs that are CYP1A2inducers should be discontinued. It is understood that such avoidingand/or discontinuing by a manufacturer, distributor, or seller ofpirfenidone can be a contraindication. In other embodiments, theinformation or recommendation may include that drugs that are CYP1A2inducers should be used with caution. In yet other embodiments, theinformation or recommendation may be any of the regimens for titratingthe dosage of pirfenidone administered to a patient upward relative to apreviously administered dosage in the patient, as described above.

The package insert, package label, instructions or other labeling mayfurther comprise directions for treating IPF by administeringpirfenidone, e.g., at a dosage of at least 1800 mg, or 2400 mg or 2403mg per day.

In related aspect, the invention provides a method of preparing orpackaging a pirfenidone medicament comprising packaging pirfenidone,optionally in a container, together with a package insert or packagelabel or instructions including any one, two, three or more of theforegoing information or recommendations.

In some embodiments, a method of treating IPF is disclosed comprisingproviding, selling or delivering any of the kits of disclosed herein toa hospital, physician or patient.

The invention will be more fully understood by reference to thefollowing examples which detail exemplary embodiments of the invention.They should not, however, be construed as limiting the scope of theinvention. All citations throughout the disclosure are hereby expresslyincorporated by reference.

EXAMPLES

An open-label Phase 1 study was performed to determine the impacts of astrong CYP1A2 inhibitor and a CYP1A2 inducer on the pharmacokinetics andsafety of pirfenidone in healthy subjects.

Study Design.

The study was a Phase 1, open-label, parallel-group study designed toinvestigate the impact of CYP1A2 inhibition and induction on thepharmacokinetics and safety of pirfenidone in healthy subjects.Fifty-four subjects were to be enrolled in two groups, consisting of 27subjects who were smokers (Group 1) and 27 subjects who were nonsmokers(Group 2). Each group (smokers and nonsmokers) was to include a minimumof nine females and nine males, and attempts were to be made to enrollequal numbers of each sex in each group. Each subject was to receive asingle 801-mg dose of pirfenidone on Days 1 and 11. Fluvoxamine dosingwas started on Day 2 and titrated to the final dose according to thefollowing schedule:

-   -   Days 2-4: fluvoxamine 50 mg at bedtime    -   Days 5-7: fluvoxamine 50 mg twice a day (in the morning and at        bedtime)    -   Days 8-11: fluvoxamine 50 mg in the morning and 100 mg at        bedtime

All pharmacokinetic (PK) analyses were conducted using population PKmethods using Monte-Carlo parametric expectation maximization asimplemented in the open-source software program S ADAPT 1.5.6 (Bauer etal., AAPS Journal 9 (1):E60-83, 2007). The structural model for theanalysis was obtained from a preliminary population PK analysis. Thispopulation PK model was fit to the pirfenidone and 5 carboxy-pirfenidoneplasma concentration-time data from Days 1 and 11 separately. Once afinal population PK model was defined, AUC_(0-∞) estimates weregenerated by simulating plasma PK profiles and compared forstatistically significant differences between days (to test the effectof fluvoxamine co-administration) and between groups (to test the effectof smoking).

As the primary endpoint of the study, differences in the pirfenidone and5 carboxy pirfenidone AUC_(0-∞) estimates between Days 1 and 11, andbetween smokers and nonsmokers were tested for significance. Theanalysis of the effect of fluvoxamine (i.e., Day 1 versus Day 11) wasanalyzed using the FDA criteria for bioequivalence for paired data (FDA2003). The ratio of AUC_(0-∞) on Day 11 to that on Day 1 was used totest for the interaction between smoking status and fluvoxaminecoadministration. If other subject characteristics (such as body size orage) were also associated with the ratio of AUC_(0-∞) on Day 11 to thaton Day 1, the significance of these covariates was also tested. Thesignificance of differences in pirfenidone and 5-carboxy-pirfenidoneAUC_(0-∞) estimates on Day 1 in smokers and nonsmokers was tested usingmultivariable linear regression in order to take into account theeffects of other significant covariates.

Pharmacokinetic Results.

Fifty-one of the 54 subjects enrolled in the study were included in thePK analyses. Three subjects were removed from the PK analyses as theydid not meet the protocol-specified requirement for adequate compliancewith the fluvoxamine dosing regimen. Two subjects discontinued the studyearly due to adverse events, and one subject only took 73% of theprotocol-required fluvoxamine dose. All 51 subjects had the fullcomplement of PK samples available for analysis. Each subject had twoprofiles on each day: one for pirfenidone and one for 5 carboxypirfenidone. There were a total of 1224 samples (12 per subject perday); each sample was assayed for pirfenidone and 5 carboxy-pirfenidonefor a total of 2448 concentrations.

A robust fit to the data was obtained using the population PK structuralmodel. In general, the fits of the data were excellent: 98% of theindividual profiles had r² values above 0.9 and there was no systematicbias in the fits.

The summary statistics of AUC_(0-∞) stratified by study day are providedin Table 1. Symmetrical dot density plots of pirfenidone and 5 carboxypirfenidone AUC_(0-∞) values versus study day, identified by smokingstatus, are provided in FIG. 2.7.2-3. The co-administration offluvoxamine resulted in a significant increase in the AUC_(0-∞) ofpirfenidone (p<0.00001). There was not a statistically significanteffect of fluvoxamine co-administration on 5 carboxy pirfenidoneAUC_(0-∞).

TABLE 1 Comparison of AUC_(0-∞) Between Study Days (n = 51) AUC_(0-∞)(mg · hr/L) 5-Carboxy- Study Day Statistic Pirfenidone^(a)Pirfenidone^(b) 1: Pre- Mean (SD) 34.9 (16.9) 29.3 (8.22) FluvoxamineMedian (25^(th)-75^(th)) 34.7 (21.4-45.9) 26.9 (22.0-33.7) 11: Post-Mean (SD)  171 (47.7) 31.7 (8.96) Fluvoxamine Median (25^(th)-75^(th)) 167 (126-206) 29.4 (25.4-36.5) ^(a)p-value <0.00001 (paired t-test)^(b)p-value = 0.168 (paired t-test) AUC_(0-∞) = area under theconcentration-time curve from time zero to infinity; SD = standarddeviation.

There was also a large apparent difference in the C_(max) estimates pre-and post-fluvoxamine; the pirfenidone C_(max) was higher afteradministration of fluvoxamine while the 5 carboxy pirfenidone C_(max)was lower after administration of fluvoxamine. The mean (95% CI) for theratio of C_(max) on Day 11 to the C_(max) on Day 1 was 2.09 (1.94-2.25)for pirfenidone and 0.369 (0.349-0.390) for 5-carboxy-pirfenidone.

The summary statistics of the ratio of the AUC_(0-∞) on Day 11 to theAUC_(0-∞) on Day 1, stratified by smoking status, are provided in Table2. While both smokers and nonsmokers were affected by thecoadministration of fluvoxamine, smokers appeared to have a morepronounced increase in exposure to pirfenidone, as evidenced by thehigher ratio of Day 11 to Day 1 AUC. Given that there was an imbalancein the demographics between smokers and nonsmokers (smokers wereyounger, heavier and predominantly male), the impact of these variableson the ratio of the pirfenidone AUC_(0-∞) on Day 11 to the AUC_(0-∞) onDay 1 was tested using multiple linear regression. Using backwardelimination (p-value for removal=0.10), smoking status was the onlysignificant predictor of the ratio of the pirfenidone AUC_(0-∞) on Day11 to the AUC_(0-∞) on Day 1; body size, sex, and age were notsignificant.

TABLE 2 Comparison of Ratio of Day 11 AUC_(0-∞) to Day 1 AUC_(0-∞) bySmoking Status Smoking Status Statistic Pirfenidone5-Carboxy-Pirfenidone Smokers N 26 26 Mean (SD) 7.32 (2.12) 1.12(0.0951) Median 7.07 (6.12-8.25) 1.13 (1.04-1.19) (25^(th)-75^(th))Nonsmokers N 25 25 Mean (SD) 4.13 (1.15) 1.05 (0.114) Median 3.99(3.26-4.68) 1.03 (0.978-1.11) (25^(th)-75^(th)) AUC_(0-∞) = area underthe concentration-time curve from time zero to infinity; SD = standarddeviation.

The relationship between smoking status and exposure to pirfenidone and5 carboxy pirfenidone were examined using the AUC_(0-∞) estimates fromDay 1. Due to the high degree of correlation between BSA and otherdemographic variables (sex, creatinine clearance (mL/min) (CLcr), age)and the pharmacologic plausibility of a relationship between exposureand body size, AUC_(0-∞) was first normalized to body surface areabefore application of multiple linear regression. Smoking status was theonly significant predictor of the variability in pirfenidone AUC_(0-∞)normalized to BSA. Smoking status had a pronounced effect in thatsmokers would be predicted to have a ˜50% drop in AUC_(0-∞) afteraccounting for differences in BSA. For 5 carboxy-pirfenidone AUC_(0-∞),the only significant predictors were age and CLcr.

In summary, the design and execution of this study allowed for a robustand informative analysis of the effects of CYP1A2 inhibition and/orinduction on the pharmacokinetics of pirfenidone. Administration of thepotent CYP inhibitor fluvoxamine resulted in a significant druginteraction and markedly increased pirfenidone exposure. Smokers werelikely to experience significantly lower pirfenidone exposure (in theabsence of the drug interaction) presumably due to the inductive effectsof smoking.

The coadministration of fluvoxamine resulted in a significant druginteraction such that exposure (AUC_(0-∞)) to pirfenidone was, onaverage, nearly 6 times higher after ten days of dosing with fluvoxamineSubjects also experienced, on average, a two-fold increase in C_(max)after administration of fluvoxamine.

Administration of pirfenidone to patients who smoke resulted in asignificant decrease in exposure (AUC_(0-∞)) to pirfenidone, and was, onaverage, about 50% the exposure of pirfenidone in patients that didn'tsmoke.

While the present invention has been described in terms of variousembodiments and examples, it is understood that variations andimprovements will occur to those skilled in the art. Therefore, onlysuch limitations as appear in the claims should be placed on theinvention.

Examples of Embodiments of the Invention Include

1. A method of administering pirfenidone therapy to a patient in needthereof comprising administering to the patient a therapeuticallyeffective amount of pirfenidone and avoiding use or administration of astrong inducer of a cytochrome P450 (CYP) that metabolizes pirfenidone.

2. The method of paragraph 1, wherein the strong inducer of CYP isavoided for at least 2.5 hours after administration of the pirfenidone.

3. The method of paragraph 2, wherein the patient is a smoker and avoidssmoking for at least 2.5 hours after administration of the pirfenidone.

4. A method of administering pirfenidone therapy to a patient in needthereof, wherein the patient is receiving an inducer of a cytochromeP450 (CYP) that metabolizes pirfenidone, comprising discontinuing use oradministration of the inducer of a cytochrome P450 (CYP) thatmetabolizes pirfenidone to avoid an adverse drug reaction andadministering a therapeutically effective amount of pirfenidone.

5. The method of paragraph 4, wherein the inducer of CYP is discontinuedprior to administration of pirfenidone.

6. The method of paragraph 5, wherein the inducer of CYP is discontinuedwithin 4 weeks prior to the administration of pirfenidone.

7. The method of paragraph 4, wherein the inducer of CYP is discontinuedconcurrent to administration of pirfenidone.

8. The method of paragraph 1 or 4, wherein the patient is a smoker,comprising discontinuing smoking.

9. The method of paragraph 8, further comprising administering anicotine replacement therapy to the patient.

10. The method of paragraph 9, wherein the nicotine replacement therapycomprises one or more of a nicotine patch, a nicotine gum, a nicotinelozenge, a nicotine nasal spray, and a nicotine inhaler.

11. The method of paragraph 8, further comprising administering to thepatient bupropion hydrochloride (Zyban) or varenicline (Chantix).

12. A method of administering pirfenidone therapy to a patient in needthereof, comprising administering to the patient a therapeuticallyeffective amount of pirfenidone, and any one or more of the following:

-   -   (a) advising the patient that strong inducers of a cytochrome        P450 (CYP) that metabolizes pirfenidone should be avoided or        discontinued;    -   (b) advising the patient that smoking should be avoided or        discontinued;    -   (c) advising the patient that co-administration of pirfenidone        with an inducer of CYP that metabolizes pirfenidone can alter        the therapeutic effect of pirfenidone;    -   (d) advising the patient that administration of pirfenidone in        patients that smoke results in a 50% decrease in pirfenidone        exposure compared to patients that do not smoke; and    -   (e) advising the patient that smoking may result in decreased        pirfenidone exposure due to the potential for smoking to induce        CYP1A2 metabolism.

13. The method of paragraph 12, wherein the patient is a smoker, andfurther comprising advising the patient to consider nicotine replacementtherapy in place of smoking.

14. The method of any one of paragraphs 12-13, further comprisingencouraging patients who smoke to stop smoking before treatment withpirfenidone.

15. The method of any one of paragraphs 1-14, wherein thetherapeutically effective amount of pirfenidone is a total daily dose ofabout 2400 mg.

16. The method of any one of paragraphs 1-15, wherein the pirfenidone isadministered three times a day, at a total daily dose of about 2400 mg.

17. The method of any one of paragraphs 1-16, wherein the CYP comprisesCYP1A2.

18. The method of any one of paragraphs 1-17, wherein the patientsuffers from idiopathic pulmonary fibrosis (IPF).

19. The method of any one of paragraphs 1-18, wherein the pirfenidone isco-administered with food.

20. The method of any one of paragraphs 1-19, wherein the inducer of acytochrome P450 (CYP) that metabolizes pirfenidone is one or more ofcarbamazepine, charbroiled food, cigarette smoke, cruciferousvegetables, esomeprazole, griseofulvin, insulin, lansprazole, marijuanasmoke, moricizine, omeprazole, phenobarbital, phenyloin, primidonerifampin, ritonavir, smoking, and St. John's wort.

Other Examples of Embodiments of the Invention Include

1A. A method of administering pirfenidone therapy to a patient in needthereof, wherein the patient is a smoker, comprising discontinuingsmoking to avoid an adverse drug reaction and administering atherapeutically effective amount of pirfenidone.2A. The method of paragraph 1A, wherein the patient discontinues smokingwithin 4 weeks prior to the administration of pirfenidone.3A. The method of paragraph 1A, wherein the patient discontinues smokingconcurrent to administration of pirfenidone.4A. The method of paragraph 1A, comprising discontinuing smoking toavoid an adverse drug reaction which is decreased exposure topirfenidone.5A. The method of paragraph 1A, further comprising advising the patientthat administration of pirfenidone in patients that smoke results in a50% decrease in pirfenidone exposure compared to patients that do notsmoke.6A. The method of paragraph 1A, wherein the patient has idiopathicpulmonary fibrosis.7A. The method of paragraph 1A, wherein the therapeutically effectiveamount of pirfenidone is 2400 mg or 2403 mg per day.8A. A method of administering pirfenidone therapy to a patient in needthereof comprising administering to the patient a therapeuticallyeffective amount of pirfenidone and avoiding use or administration of astrong inducer of a cytochrome P450 1A2 (CYP1A2) to avoid an adversedrug reaction.9A. The method of paragraph 8A, comprising avoiding use oradministration of a strong inducer of CYP1A2 to avoid an adverse drugreaction which is reduced exposure to pirfenidone.10A. The method of paragraph 8A, wherein the patient is a smoker andavoids smoking when using pirfenidone.11A. The method of paragraph 8A, wherein the patient has idiopathicpulmonary fibrosis.12A. The method of paragraph 8A, wherein the therapeutically effectiveamount of pirfenidone is 2400 mg or 2403 mg per day.13A. A method of administering pirfenidone therapy to a patient in needthereof, comprising administering to the patient a therapeuticallyeffective amount of pirfenidone, and one or more of the following:

-   -   (a) advising the patient that inducers of a cytochrome P450        (CYP) (CYP1A2) should be avoided or discontinued;    -   (b) advising the patient that smoking should be avoided when        using pirfenidone due to the potential for smoking to induce        CYP1A2 metabolism resulting in decreased exposure to        pirfenidone;    -   (c) advising the patient that smoking should be discontinued        before treatment with pirfenidone;    -   (d) advising the patient that administration of pirfenidone in        patients that smoke results in a 50% decrease in pirfenidone        exposure compared to patients that do not smoke; and    -   (e) advising the patient that smoking may result in decreased        pirfenidone exposure due to the potential for smoking to induce        CYP1A2 metabolism.        14A. The method of paragraph 13A, further comprising encouraging        patients who smoke to stop smoking before treatment with        pirfenidone.        15A. The method of paragraph 13A, expedient (a), comprising        advising the patient that strong inducers of a CYP1A2 should be        avoided or discontinued.        16A. The method of paragraph 13A, wherein the inducer of a        CYP1A2 is one or more of carbamazepine, charbroiled food,        cigarette smoke, cruciferous vegetables, esomeprazole,        griseofulvin, insulin, lansprazole, marijuana smoke, moricizine,        omeprazole, phenobarbital, phenyloin, primidone rifampin,        ritonavir, smoking, and St. John's wort.        17A. The method of paragraph 16A, wherein the CYP1A2 inducer is        selected from the group consisting of carbamazepine,        esomeprazole, griseofulvin, insulin, lansprazole, moricizine,        omeprazole, rifampin, ritonavir, and smoking.        18A. The method of paragraph 16A, wherein the CYP1A2 inducer is        selected from the group consisting of carbamazepine,        lansoprazole, omeprazole, phenobarbital, phenyloin, primidone,        rifampin, ritonavir, smoking, and St. John's wort.        19A. The method of paragraph 13A, wherein the patient in need of        pirfenidone therapy is treated for idiopathic pulmonary        fibrosis.        20A. The method of paragraph 13A, wherein the therapeutically        effective amount of pirfenidone is 2400 mg or 2403 mg per day.

Still Other Examples of Embodiments of the Invention Include

1B. Pirfenidone for use in treating a patient in need of pirfenidonetherapy, characterized in that the treating comprises avoiding ordiscontinuing concomitant use or co-administration of a strong inducerof cytochrome P450 1A2 (CYP1A2) to avoid reduced exposure topirfenidone.2B. The use of pirfenidone in the manufacture of a medicament fortreating a patient in need of pirfenidone therapy, characterized in thatthe treating comprises avoiding or discontinuing concomitant use orco-administration of a strong inducer of cytochrome P450 1A2 (CYP1A2) toavoid reduced exposure to pirfenidone.3B. The pirfenidone or use of any one of paragraphs 1B to 2Bcharacterized in that the treating comprises avoiding concomitant use orco-administration of a strong inducer of cytochrome P450 1A2 (CYP1A2).4B. The pirfenidone or use of any one of paragraphs 1B to 2B wherein thepatient is avoiding concomitant use or co-administration of a stronginducer of cytochrome P450 1A2 (CYP1A2).5B. The pirfenidone or use of any one of paragraphs 1B to 2B wherein thepatient is a smoker who is discontinuing smoking to avoid reducedexposure to pirfenidone.6B. The pirfenidone or use of paragraph 5B wherein the patient isdiscontinuing smoking within 4 weeks prior to the administration ofpirfenidone.7B. The pirfenidone or use of paragraph 5B wherein the patient isdiscontinuing smoking concurrent with the start of administration ofpirfenidone.8B. The pirfenidone or use of any one of paragraphs 1B to 2B wherein thepatient is a smoker and avoids smoking when using pirfenidone.9B. The pirfenidone or use of any one of paragraphs 1B to 4B wherein theinducer of a CYP1A2 is one or more of carbamazepine, charbroiled food,cigarette smoke, cruciferous vegetables, esomeprazole, griseofulvin,insulin, lansprazole, marijuana smoke, moricizine, omeprazole,phenobarbital, phenyloin, primidone rifampin, ritonavir, smoking, andSt. John's wort.10B. The pirfenidone or use of any one of paragraphs 1B to 9B whereinthe patient suffers from a disease selected from pulmonary fibrosis,idiopathic pulmonary fibrosis, idiopathic interstitial pneumonia,autoimmune lung diseases, benign prostate hypertrophy, coronary ormyocardial infarction, atrial fibrillation, cerebral infarction,myocardiac fibrosis, musculoskeletal fibrosis, post-surgical adhesions,liver cirrhosis, renal fibrotic disease, fibrotic vascular disease,scleroderma, Hermansky-Pudlak syndrome, neurofibromatosis, Alzheimer'sdisease, diabetic retinopathy, or skin lesions, lymph node fibrosisassociated with HIV, chronic obstructive pulmonary disease (COPD),inflammatory pulmonary fibrosis, rheumatoid arthritis; rheumatoidspondylitis; osteoarthritis; gout, other arthritic conditions; sepsis;septic shock; endotoxic shock; gram-negative sepsis; toxic shocksyndrome; myofacial pain syndrome (MPS); Shigellosis; asthma; adultrespiratory distress syndrome; inflammatory bowel disease; Crohn'sdisease; psoriasis; eczema; ulcerative colitis; glomerular nephritis;scleroderma; chronic thyroiditis; Grave's disease; Ormond's disease;autoimmune gastritis; myasthenia gravis; autoimmune hemolytic anemia;autoimmune neutropenia; thrombocytopenia; pancreatic fibrosis; chronicactive hepatitis including hepatic fibrosis; acute or chronic renaldisease; renal fibrosis; diabetic nephropathy; irritable bowel syndrome;pyresis; restenosis; cerebral malaria; stroke or ischemic injury; neuraltrauma; Alzheimer's disease; Huntington's disease; Parkinson's disease;acute or chronic pain; allergies, including allergic rhinitis orallergic conjunctivitis; cardiac hypertrophy, chronic heart failure;acute coronary syndrome; cachexia; malaria; leprosy; leishmaniasis; Lymedisease; Reiter's syndrome; acute synoviitis; muscle degeneration,bursitis; tendonitis; tenosynoviitis; herniated, ruptured, or prolapsedintervertebral disk syndrome; osteopetrosis; thrombosis; silicosis;pulmonary sarcosis; bone resorption diseases, such as osteoporosis ormultiple myeloma-related bone disorders; cancer, including but notlimited to metastatic breast carcinoma, colorectal carcinoma, malignantmelanoma, gastric cancer, or non-small cell lung cancer;graft-versus-host reaction; or auto-immune diseases, such as multiplesclerosis, lupus or fibromyalgia; AIDS or other viral diseases such asHerpes Zoster, Herpes Simplex I or II, influenza virus, Severe AcuteRespiratory Syndrome (SARS) or cytomegalovirus; or diabetes mellitus,proliferative disorders (including both benign or malignanthyperplasias), acute myelogenous leukemia, chronic myelogenous leukemia,Kaposi's sarcoma, metastatic melanoma, multiple myeloma, breast cancer,including metastatic breast carcinoma; colorectal. carcinoma; malignantmelanoma; gastric cancer; non-small cell lung cancer (NSCLC); bonemetastases; pain disorders including neuromuscular pain, headache,cancer pain, dental pain, or arthritis pain; angiogenic disordersincluding solid tumor angiogenesis, ocular neovascularization, orinfantile hemangioma; conditions associated with the cyclooxygenase orlipoxygenase signaling pathways, including conditions associated withprostaglandin endoperoxide synthase-2 (including edema, fever,analgesia, or pain); organ hypoxia; thrombin-induced plateletaggregation; or protozoal diseases.11B. The pirfenidone or use of any one of paragraphs 1B to 10B whereinthe patient has idiopathic pulmonary fibrosis.12B. The pirfenidone or use of any one of paragraphs 1B to 11B whereinthe pirfenidone is administered at a total daily dosage of 2400 mg or2403 mg per day.13B. The pirfenidone or use of any one of paragraphs 1B to 12B, whereineach dose of pirfenidone administered is 801 mg.14B. Pirfenidone for use in treating a patient in need of pirfenidonetherapy, characterized in that the treating comprises administeringpirfenidone to the patient and contraindicating, avoiding ordiscontinuing a strong inducer of cytochrome P450 1A2 (CYP1A2) to avoidreduced exposure to pirfenidone.15B. A package or kit comprising (a) pirfenidone, optionally in acontainer, and (b) a package insert, package label, instructions orother labeling comprising contraindicating, avoiding, or discontinuingconcomitant use or co-administration of a strong inducer of cytochromeP450 1A2 (CYP1A2), and optionally according to any of the embodiments ofparagraphs 1B-14B or as described anywhere above.

1. (canceled)
 2. (canceled)
 3. A method of administering pirfenidonetherapy to a patient in need thereof comprising administering to thepatient a therapeutically effective amount of pirfenidone and avoidingor discontinuing a strong inducer of a cytochrome P450 1A2 (CYP1A2) toavoid reduced exposure to pirfenidone.
 4. The method of claim 3comprising avoiding concomitant use or co-administration of a strongCYP1A2 inducer.
 5. The method of claim 3 comprising discontinuing astrong CYP1A2 inducer prior to or concurrent with starting pirfenidonetherapy to avoid reduced exposure to pirfenidone.
 6. The method of claim3 wherein the patient is a smoker who is discontinuing smoking to avoidreduced exposure to pirfenidone.
 7. The method of claim 6 wherein thepatient is discontinuing smoking within 4 weeks prior to theadministration of pirfenidone.
 8. The method of claim 7 wherein thepatient is discontinuing smoking concurrent with the start ofadministration of pirfenidone.
 9. The method of claim 3 wherein thepatient is a smoker and avoids smoking when using pirfenidone.
 10. Themethod of claim 3 wherein the strong CYP1A2 inducer is rifampin.
 11. Themethod of claim 3 wherein the patient has idiopathic pulmonary fibrosis.12. The method of claim 3 wherein the patient suffers from a diseaseselected from pulmonary fibrosis, idiopathic pulmonary fibrosis,idiopathic interstitial pneumonia, autoimmune lung diseases, benignprostate hypertrophy, coronary or myocardial infarction, atrialfibrillation, cerebral infarction, myocardiac fibrosis, musculoskeletalfibrosis, post-surgical adhesions, liver cirrhosis, renal fibroticdisease, fibrotic vascular disease, scleroderma, Hermansky-Pudlaksyndrome, neurofibromatosis, Alzheimer's disease, diabetic retinopathy,or skin lesions, lymph node fibrosis associated with HIV, chronicobstructive pulmonary disease (COPD), inflammatory pulmonary fibrosis,rheumatoid arthritis; rheumatoid spondylitis; osteoarthritis; gout,other arthritic conditions; sepsis; septic shock; endotoxic shock;gram-negative sepsis; toxic shock syndrome; myofacial pain syndrome(MPS); Shigellosis; asthma; adult respiratory distress syndrome;inflammatory bowel disease; Crohn's disease; psoriasis; eczema;ulcerative colitis; glomerular nephritis; scleroderma; chronicthyroiditis; Grave's disease; Ormond's disease; autoimmune gastritis;myasthenia gravis; autoimmune hemolytic anemia; autoimmune neutropenia;thrombocytopenia; pancreatic fibrosis; chronic active hepatitisincluding hepatic fibrosis; acute or chronic renal disease; renalfibrosis; diabetic nephropathy; irritable bowel syndrome; pyresis;restenosis; cerebral malaria; stroke or ischemic injury; neural trauma;Alzheimer's disease; Huntington's disease; Parkinson's disease; acute orchronic pain; allergies, including allergic rhinitis or allergicconjunctivitis; cardiac hypertrophy, chronic heart failure; acutecoronary syndrome; cachexia; malaria; leprosy; leishmaniasis; Lymedisease; Reiter's syndrome; acute synoviitis; muscle degeneration,bursitis; tendonitis; tenosynoviitis; herniated, ruptured, or prolapsedintervertebral disk syndrome; osteopetrosis; thrombosis; silicosis;pulmonary sarcosis; bone resorption diseases, such as osteoporosis ormultiple myeloma-related bone disorders; cancer, including but notlimited to metastatic breast carcinoma, colorectal carcinoma, malignantmelanoma, gastric cancer, or non-small cell lung cancer;graft-versus-host reaction; or auto-immune diseases, such as multiplesclerosis, lupus or fibromyalgia; AIDS or other viral diseases such asHerpes Zoster, Herpes Simplex I or II, influenza virus, Severe AcuteRespiratory Syndrome (SARS) or cytomegalovirus; or diabetes mellitus,proliferative disorders (including both benign or malignanthyperplasias), acute myelogenous leukemia, chronic myelogenous leukemia,Kaposi's sarcoma, metastatic melanoma, multiple myeloma, breast cancer,including metastatic breast carcinoma; colorectal, carcinoma; malignantmelanoma; gastric cancer; non-small cell lung cancer (NSCLC); bonemetastases; pain disorders including neuromuscular pain, headache,cancer pain, dental pain, or arthritis pain; angiogenic disordersincluding solid tumor angiogenesis, ocular neovascularization, orinfantile hemangioma; conditions associated with the cyclooxygenase orlipoxygenase signaling pathways, including conditions associated withprostaglandin endoperoxide synthase-2 (including edema, fever,analgesia, or pain); organ hypoxia; thrombin-induced plateletaggregation; or protozoal diseases.
 13. The method of claim 3 whereinthe pirfenidone is administered at a total daily dosage of at least 1800mg.
 14. The method of claim 13 wherein the pirfenidone is administeredat a total daily dosage of 2400 mg or 2403 mg.
 15. The method of claim3, wherein each dose of pirfenidone administered is 801 mg.
 16. Themethod of claim 3, wherein pirfenidone is administered three times aday.
 17. The method of claim 3, wherein pirfenidone is administered withfood.
 18. (canceled)